MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
  Most Studied  CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO
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expandhemorrhagic disorder due to an acquired platelet anomaly (MONDO:0016631)
Parent Node:
expandsystemic disease (MONDO:0015938)
..Starting node
..expandTAFRO syndrome ()

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 Sister Nodes: 
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..expandcapillary leak syndrome ()
..expandconnective tissue disorder due to lysyl hydroxylase-3 deficiency ()
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..expandretinal ischemic syndrome-digestive tract small vessel hyalinosis-diffuse cerebral calcifications syndrome ()
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..expandsarcoidosis ()
..expandsystemic autoimmune disease ()
..expandsystemic disease with cataract ()
..expandsystemic disease with skin involvement ()
..expandsystemic diseases with anterior uveitis ()
..expandsystemic diseases with panuveitis ()
..expandsystemic diseases with posterior uveitis ()
..expandTAFRO syndrome ()
..expandtempi syndrome ()
..expandunexplained long-lasting fever/inflammatory syndrome ()
..expandX-linked reticulate pigmentary disorder ()
   

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Further data from MedGen, OMIM,ClinVar, CTD
Term ID:18702
Name:TAFRO syndrome
Definition:A clinicopathologic variant of multicentric Castleman's disease characterized by thrombocytopenia, ascites (anasarca), microcytic anemia, myelofibrosis, renal dysfunction, and organomegaly
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Synonyms:Castleman-Kojima disease; thrombocytopenia-anasarca-fever-renal insufficiency-organomegaly syndrome
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal